US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Apr 8, 2026 (5 months ago)

TRIFLUENT PHARMA TRIDERGEL Wound Care Gel, (Benzalkonium Chloride 0.1%), 1.0 fl oz, (29.6…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated

What was recalled

TRIFLUENT PHARMA TRIDERGEL Wound Care Gel, (Benzalkonium Chloride 0.1%), 1.0 fl oz, (29.6 mL) bottle with long pointy cap, Manufactured for: Trifluent Pharma, LLC. San Antonio, TX 78213. NDC 73352-520-01.

Recalling firm
Blaine Labs Inc
NDC code
73352-520-01
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0693-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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